Perfluorooctane sulfonate aggravates CCl4 ‐induced hepatic fibrosis via HMGB1 / TLR4 /Smad signaling

2022 ◽  
Author(s):  
Chunhua Wan ◽  
Tianye Gu ◽  
Junyi Ling ◽  
Yi Qin ◽  
Jiashan Luo ◽  
...  
Keyword(s):  
Hepatic Fibrosis ◽  
Perfluorooctane Sulfonate ◽  
Smad Signaling

scholarly journals The polysaccharides from Grifola frondosa attenuate CCl4-induced hepatic fibrosis in rats via the TGF-β/Smad signaling pathway

RSC Advances ◽  
2019 ◽  
Vol 9 (58) ◽  
pp. 33684-33692 ◽  
Author(s):  
Chao Li ◽  
Meng Meng ◽  
Mingzhu Guo ◽  
Mengyang Wang ◽  
Aining Ju ◽  
...  
Keyword(s):  
Signaling Pathway ◽  
Hepatic Fibrosis ◽  
Grifola Frondosa ◽  
Smad Signaling ◽  
Smad Signaling Pathway ◽  
Tgf Β1

The TGF-β1/Smad signaling pathway has been linked to hepatic fibrosis.

scholarly journals Effect of Oxymatrine on the TGFbeta-Smad signaling pathway in rats with CCl4-induced hepatic fibrosis

2008 ◽  
Vol 14 (13) ◽  
pp. 2100 ◽  
Author(s):  
Xiao-Ling Wu ◽  
Wei-Zheng Zeng ◽  
Ming-De Jiang ◽  
Jian-Ping Qin ◽  
Hui Xu
Keyword(s):  
Signaling Pathway ◽  
Hepatic Fibrosis ◽  
Smad Signaling ◽  
Smad Signaling Pathway

scholarly journals Honokiol Acts as a Potent Anti-Fibrotic Agent in the Liver through Inhibition of TGF-β1/SMAD Signaling and Autophagy in Hepatic Stellate Cells

2021 ◽  
Vol 22 (24) ◽  
pp. 13354
Author(s):  
Seita Kataoka ◽  
Atsushi Umemura ◽  
Keiichiro Okuda ◽  
Hiroyoshi Taketani ◽  
Yuya Seko ◽  
...  
Keyword(s):  
Liver Fibrosis ◽  
Signaling Pathway ◽  
Hepatic Fibrosis ◽  
Hepatic Stellate Cells ◽  
Stellate Cells ◽  
Smad Signaling ◽  
Smad Signaling Pathway ◽  
Tgf Β1

Chronic liver injury may result in hepatic fibrosis, which can progress to cirrhosis and eventually liver failure. There are no drugs that are specifically approved for treating hepatic fibrosis. The natural product honokiol (HNK), a bioactive compound extracted from Magnolia grandiflora, represents a potential tool in the management of hepatic fibrosis. Though HNK has been reported to exhibit suppressive effects in a rat fibrosis model, the mechanisms accounting for this suppression remain unclear. In the present study, the anti-fibrotic effects of HNK on the liver were evaluated in vivo and in vitro. In vivo studies utilized a murine liver fibrosis model, in which fibrosis is induced by treatment with carbon tetrachloride (CCl4). For in vitro studies, LX-2 human hepatic stellate cells (HSCs) were treated with HNK, and expression of markers of fibrosis, cell viability, the transforming growth factor-β (TGF-β1)/SMAD signaling pathway, and autophagy were analyzed. HNK was well tolerated and significantly attenuated CCl4-induced liver fibrosis in vivo. Moreover, HNK decreased HSC activation and collagen expression by downregulating the TGF-β1/SMAD signaling pathway and autophagy. These results suggest that HNK is a new potential candidate for the treatment of hepatic fibrosis through suppressing both TGF-β1/SMAD signaling and autophagy in HSCs.

scholarly journals Astragaloside Inhibits Hepatic Fibrosis by Modulation of TGF-β1/Smad Signaling Pathway

2018 ◽  
Vol 2018 ◽  
pp. 1-13 ◽  
Author(s):  
Xingxing Yuan ◽  
Zhiqiang Gong ◽  
Bingyu Wang ◽  
Xueying Guo ◽  
Lei Yang ◽  
...  
Keyword(s):  
Signaling Pathway ◽  
Hepatic Fibrosis ◽  
Collagen Fibers ◽  
Control Group ◽  
Smad Signaling ◽  
Smad Proteins ◽  
Smad Signaling Pathway ◽  
Smad 3

Activation of HSC is a pivotal step in hepatic fibrosis. In the activation of HSC, the TGF-β1 plays a key role that can promote the occurrence of hepatic fibrosis by combining with Smad proteins. Astragaloside is the main active component extracted from Radix Astragali that has the effect of antioxidation and hepatoprotection. In the present study, we investigated the mechanism of astragalosides inhibiting hepatic fibrosis in vitro and in vivo. In vitro, astragalosides inhibited the activation of HSC and regulated the expression of MMP-2 and TIMP-2 and reduced the formation of collagen fibers. In vivo, administration of astragalosides decreased the serum ALT, AST, and TBiL in rats by reducing oxidative stress. Astragalosides also attenuated hepatic fibrosis by reducing the concentration of hydroxyproline and inhibiting the formation of collagen fibers. The expressions of TGF-β1, TβR-I, p-Smad 2, and p-Smad 3 were downregulated after astragalosides treatments, while Smad 7 was upregulated compared to the control group. The results indicated that the effect of astragaloside on hepatic fibrosis was related to the inhibition of HSC activation and the modulation of the TGF-β1/Smad signaling pathway.

San-Cao Granule (三草颗粒) Ameliorates Hepatic Fibrosis through High Mobility Group Box-1 Protein/Smad Signaling Pathway

2015 ◽  
Vol 24 (7) ◽  
pp. 502-511 ◽  
Author(s):  
Shi-zhang Wei ◽  
Sheng-qiang Luo ◽  
Jian Wang ◽  
Jia-bo Wang ◽  
Rui-sheng Li ◽  
...  
Keyword(s):  
Signaling Pathway ◽  
Hepatic Fibrosis ◽  
High Mobility ◽  
High Mobility Group ◽  
Smad Signaling ◽  
Smad Signaling Pathway
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